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New transformation of cycloalkanone acetals by peracids α,ω-dicarboxylic acids synthesis Научная публикация

Журнал Open Chemistry
ISSN: 2391-5420
Вых. Данные Год: 2005, Том: 3, Номер: 3, Страницы: 417-431 Страниц : 15 DOI: 10.2478/bf02479272
Авторы Terent'ev Alexander 1 , Chodykin Sergey 1
Организации
1 N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Leninsky Prospect 47, Moscow, Russia

Реферат: A new process of oxidation of cycloalkanone acetals under the action ofin situgenerated performic acid has been found. The main products of the reaction areα,ω-dicarboxylic acids obtained with the yield up to 77 % depending on the size of acetals ring. Theprocess has been explored and optimized on the example of thedodecanedioic acid synthesis (avaluable industrial product).
Библиографическая ссылка: Terent'ev A. , Chodykin S.
New transformation of cycloalkanone acetals by peracids α,ω-dicarboxylic acids synthesis
Open Chemistry. 2005. V.3. N3. P.417-431. DOI: 10.2478/bf02479272 WOS OpenAlex
Идентификаторы БД:
Web of science: WOS:000230619800005
OpenAlex: W2063275186
Цитирование в БД:
БД Цитирований
OpenAlex 7
Web of science 12
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